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Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

Flavonoids and Nod factors are key for legume plant growth and could help in sustainable farming.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

Case-only trees and random forests improve predictions of treatment effects in clinical trials.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

No link found between specific genes and female pattern hair loss.

The document concludes that sex hormones are crucial for mammalian reproduction, health, and behavior, and require more research for therapeutic use.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

Acne is caused by hormones, genetics, skin cell buildup, oil production, bacteria, and inflammation.

The document concludes that for hair and feather growth, it's better to target the environment around stem cells than the cells themselves.

Hair follicle development is controlled by interactions between skin tissues and specific molecular signals.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

Mice with damaged skin or hair follicles are more susceptible to anthrax infection.

Hair significantly shapes body identity and social interactions, influencing how we perceive and relate to our bodies.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Increased cell death and reduced cell growth in hair follicles contribute to baldness.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Notch signaling is essential for healthy skin and hair follicle maintenance.

DHT reduces a cell's ability to promote hair growth, while 3D culture without DHT improves it.